Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system.

Monnot, Sophie; Gigarel, Nadine; Samuels, David C; Burlet, Philippe; Hesters, Laetitia; Frydman, Nelly; Frydman, René; Kerbrat, Violaine; Funalot, Benoit; Martinovic, Jelena; Benachi, Alexandra; Feingold, Josué; Munnich, Arnold; Bonnefont, Jean-Paul; Steffann, Julie

Monnot, Sophie; Gigarel, Nadine; Samuels, David C; Burlet, Philippe; Hesters, Laetitia; Frydman, Nelly; Frydman, René; Kerbrat, Violaine; Funalot, Benoit; Martinovic, Jelena; Benachi, Alexandra; Feingold, Josué; Munnich, Arnold; Bonnefont, Jean-Paul; Steffann, Julie.

Affiliation

Monnot S; Université Paris-Descartes, Unité INSERM U, Hopital Necker-Enfants Malades, France.

Hum Mutat ; 32(1): 116-25, 2011 Jan.

Article in En | MEDLINE | ID: mdl-21120938

Subject(s)

DNA, Mitochondrial/genetics; Embryonic Development/genetics; Female; Fetal Development/genetics; Gene Dosage; Humans; MELAS Syndrome/embryology; MELAS Syndrome/genetics; Models, Genetic; Mutation; Pregnancy; Prenatal Diagnosis/methods; Prenatal Diagnosis/statistics & numerical data

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Embryonic Development Type of study: Diagnostic_studies Limits: Female / Humans / Pregnancy Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2011 Type: Article Affiliation country: France

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